Canonical Allele Identifier: CA1926143145

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863610A= , CM000672.2:g.87863610A= GRCh38
NC_000010.10:g.89623367A= , CM000672.1:g.89623367A= GRCh37
NC_000010.9:g.89613347A= NCBI36
NG_007466.2:g.5173A= , LRG_311:g.5173A=
NG_033079.1:g.4828T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-844A= (PTEN) ENSP00000516674.1:n.-16-844A=
ENST00000688308.1:c.-17+497A= (PTEN) ENSP00000508752.1:n.-17+497A=
ENST00000692337.1:c.52A= (MLDHR) ENSP00000509326.1:p.Thr18=
ENST00000693560.1:c.-340A= (PTEN) ENSP00000509861.1:n.-340A=
ENST00000371953.7:c.-860A= (PTEN) ENSP00000361021.3:n.-860A=
ENST00000610634.1:c.-962A= (PTEN) ENSP00000477517.1:n.-962A=
NM_000314.5:c.-859A= (PTEN) NP_000305.3:n.-859A=
NM_000314.6:c.-859A= (PTEN) NP_000305.3:n.-859A=
NM_001304717.2:c.-340A= (PTEN) NP_001291646.2:n.-340A=
NM_001304718.1:c.-1564A= (PTEN) NP_001291647.1:n.-1564A=